List of variants in gene SGCG reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000231.3(SGCG):c.803C>T (p.Pro268Leu)	rs143110015	0.00014
NM_000231.3(SGCG):c.653T>C (p.Ile218Thr)	rs202045534	0.00011
NM_000231.3(SGCG):c.455C>T (p.Thr152Ile)	rs201329880	0.00008
NM_000231.3(SGCG):c.1-3C>T	rs373335254	0.00003
NM_000231.3(SGCG):c.100C>T (p.Arg34Cys)	rs747549369	0.00001
NM_000231.3(SGCG):c.230G>C (p.Gly77Ala)	rs886043950	0.00001
NM_000231.3(SGCG):c.706G>A (p.Val236Met)	rs201788230	0.00001
NM_000231.3(SGCG):c.*2C>T
NM_000231.3(SGCG):c.438C>A (p.Asp146Glu)	rs144497243
NM_000231.3(SGCG):c.637G>T (p.Ala213Ser)	rs1883004416

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